Abstract
The thermal stability of linear alkanes, such as tetradecane, in the pyrolytic regime is enhanced by the addition of cyclo-akanes, in particular decalin. Based on the product distribution from the thermal stressing of their mixtures, decalin was found to target primary radicals, particularly by a sharp reduction in the n-alkane products in relation to that of the 1-alkene. This thermal interaction has been further examined by GC/MS analysis, which revealed the formation of alkylated intermediates of decalin that stabilizes the paraffinic species in the pyrolytic regime.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 562-564 |
| Number of pages | 3 |
| Journal | ACS Division of Fuel Chemistry, Preprints |
| Volume | 44 |
| Issue number | 3 |
| State | Published - 1999 |
All Science Journal Classification (ASJC) codes
- General Energy
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